Whitelock J, Mitchell S, Graham L, Underwood P A
CRC-Cardiac Technology, CSIRO, Division of Biomolecular Engineering, North Ryde, Australia.
Cell Biol Int. 1997 Mar;21(3):181-9. doi: 10.1006/cbir.1996.0125.
Extracellular proteoglycans (PGs) purified from cultured human arterial endothelial cells were tested for their effects on the proliferation of human vascular smooth muscle cells (VSMC). Fractions containing perlecan, the basement membrane heparan sulphate (HS) PG, the large chondrotin sulphate (CS) proteoglycan from connective tissue and other immunoreactive CS did not inhibit the proliferation of human VSMC. Native endothelial extracellular matrix, which was shown to contain the same PGs, demonstrated a pronounced stimulatory effect on the proliferation of human VSMCs. This stimulatory effect was not removed by pre-incubation of the matrix with 1 M NaCl, heparin, platelet extract or plasmin. These experiments demonstrate that PGs produced by human arterial endothelial cells do not inhibit the proliferation of VSMC. These data do not support the hypothesis that human endothelial cells, in vivo, control the activation or proliferation of VSMCs directly by the secretion of a non-proliferative molecule. Instead they support the hypothesis that the endothelial cells counteract intimal hyperplasia of VSMC indirectly by providing a barrier from activating factors in the plasma.
对从培养的人动脉内皮细胞中纯化的细胞外蛋白聚糖(PGs)进行了测试,以研究其对人血管平滑肌细胞(VSMC)增殖的影响。含有基底膜硫酸乙酰肝素(HS)蛋白聚糖(核心蛋白聚糖)、结缔组织中的大硫酸软骨素(CS)蛋白聚糖以及其他免疫反应性CS的组分并未抑制人VSMC的增殖。已证明含有相同PGs的天然内皮细胞外基质对人VSMC的增殖具有显著的刺激作用。用1M NaCl、肝素、血小板提取物或纤溶酶对基质进行预孵育并不能消除这种刺激作用。这些实验表明,人动脉内皮细胞产生的PGs不会抑制VSMC的增殖。这些数据不支持以下假设:在体内,人内皮细胞通过分泌非增殖性分子直接控制VSMC的激活或增殖。相反,它们支持以下假设:内皮细胞通过提供一道屏障来抵御血浆中的激活因子,从而间接对抗VSMC的内膜增生。